Become a Clinical Research Coordinator at Centricity Research in Vaughan. Engage with participants and ensure the highest study standards in clinical trials every day.

We're on the hunt for a dedicated Clinical Research Coordinator to manage a variety of clinical studies at our Vaughan site. Your expertise in conducting participant visits, phlebotomy, and ensuring regulatory compliance will be essential to our mission. Collaborate with a talented research team while gaining exposure to multiple therapeutic areas.

Key Responsibilities:
• Conduct clinical study visits compliant with regulations
• Safeguard participant well-being and manage adverse events
• Perform vital signs, ECGs, and sample handling




• Facilitate participant recruitment and screening processes
• Document study data accurately for regulatory bodies

Requirements:
• Bachelor’s degree in a health, science, or research field
• 3+ years coordinating clinical research studies
• Solid hands-on phlebotomy experience in Canada
• In-depth knowledge of medical terminology and GCP
• Highly organized and capable of multitasking

Join Centricity Research in Vaughan and make a difference in clinical research today.
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📌 Vaughan Clinical Research Coordinator Role (Ontario)
🏢 Centricity Research
📍 Ontario